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Results for "

this compound calcium salt

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
  • Cell Research
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    TargetMol | Cell_Research_Reagents
Gamma-Glu-Abu TFA
T201610
Gamma-Glu-AbuTFA is the TFA salt form of Gamma-Glu-Abu. This compound acts as an agonist for the calcium sensing receptor (CaSR), activating CaSR in HEK-293 cells with an EC50 of 0.21 μM.
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Levamlodipine besylate Hemipentahydrate
T204904884648-62-8
Levamlodipine besylate hemipentahydrate is the besylate hemipentahydrate salt form of Levamlodipine. It is an orally effective calcium channel blocker with antioxidative and vasodilatory properties. This compound can reduce serum malondialdehyde (MDA) levels, enhance the activity of superoxide dismutase (SOD), and alleviate oxidative stress. Levamlodipine besylate hemipentahydrate is relevant for research in vascular dementia, hypertension, and cerebrovascular diseases.
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D-myo-Inositol-1,2,4,5,6-pentaphosphate sodium salt
Ins(1,2,4,5,6)P5 sodium salt, 1,2,4,5,6-IP5 sodium salt
T212348
D-myo-Inositol-1,2,4,5,6-pentaphosphate (Ins(1,2,4,5,6)P5) sodium salt is one of several inositol polyphosphate isomers involved in signal transduction. In human Jurkat T lymphocytes, Ins(1,2,4,5,6)P5 (sodium salt) is phosphorylated by 1/3 kinase to form InsP6. This compound plays a role in calcium signaling pathways.
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D-myo-Inositol-2,4,5-triphosphate sodium salt
Ins(2,4,5)P3 sodium salt, 2,4,5-IP3 sodium salt
T212384
D-myo-Inositol-2,4,5-triphosphate (Ins(2,4,5)P3) (sodium salt) is a second messenger produced by the hydrolysis of phosphatidylinositol-4,5-bisphosphate mediated by phospholipase C. Upon binding to receptors on the endoplasmic reticulum, it can open calcium channels and raise intracellular calcium ion concentrations. It also acts as a partial agonist of rat hepatic IP3 receptors. This compound is utilized in the study of calcium signaling pathways.
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Orforglipron hemicalcium hydrate
LY3502970 hemicalcium hydrate, GLP-1 receptor agonist 1 hemicalcium hydrate
T870713008544-96-2
Orforglipron hemicalcium hydrate (LY3502970 hemicalcium hydrate; GLP-1 receptor agonist 1 hemicalcium hydrate) represents the hemicalcium hydrate form of the calcium salt of Orforglipron, an orally active agonist targeting the Glucagon-like peptide-1 receptor (GLP-1R). This compound has demonstrated efficacy in mitigating type 2 diabetes [1].
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EDTA disodium
Ethylenediaminetetraacetic acid disodium, EDTA disodium
TSH-00080139-33-3
EDTA disodium salt is a type of chelating agent formed by a central metal ion chelated with four carboxylate groups and two amino groups. This compound is capable of binding and chelating metal ions such as calcium, magnesium, and iron, making it useful across industrial, medical, and research settings. In food and beverages, it serves as a preservative; in pharmaceuticals, it acts as a stabilizer; in water treatment, it functions as a chelating agent; and in biochemical and biomedical research, it is utilized as a reagent. Furthermore, EDTA disodium salt has been studied for potential roles in treating heavy metal poisoning and cardiovascular diseases.
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7-10 days
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